Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154342893-154343165 | Rare:83 | ||||
chr1:154869450-154869680 | Rare:68 | ||||
chr1:154968000-154968226 | Rare:53 | ||||
chr1:155194684-155194827 | Common:2; Rare:47 | ||||
chr1:155227431-155227723 | Common:3; Rare:88 | ||||
chr1:155561764-155562030 | Common:1; Rare:53 | ||||
chr1:156130318-156130771 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:160208285-160208456 | Rare:29 | ||||
chr1:161530882-161531118 | Common:5; Rare:97 | ||||
chr1:167454992-167455142 | Common:1; Rare:30 | ||||
chr1:172144547-172144882 | Rare:58 | ||||
chr1:178542577-178542839 | Common:7; Rare:72 | ||||
chr1:183022393-183022702 | Common:1; Rare:56 | ||||
chr1:184630445-184630559 | Common:1; Rare:19 | ||||
chr1:184664085-184664188 | Common:2; Rare:30 |